New transformation of cycloalkanone acetals by peracids α,ω-dicarboxylic acids synthesis Научная публикация
Журнал |
Open Chemistry
ISSN: 2391-5420 |
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Вых. Данные | Год: 2005, Том: 3, Номер: 3, Страницы: 417-431 Страниц : 15 DOI: 10.2478/bf02479272 | ||
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Организации |
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Реферат:
A new process of oxidation of cycloalkanone acetals under the action ofin situgenerated performic acid has been found. The main products of the reaction areα,ω-dicarboxylic acids obtained with the yield up to 77 % depending on the size of acetals ring. Theprocess has been explored and optimized on the example of thedodecanedioic acid synthesis (avaluable industrial product).
Библиографическая ссылка:
Terent'ev A.
, Chodykin S.
New transformation of cycloalkanone acetals by peracids α,ω-dicarboxylic acids synthesis
Open Chemistry. 2005. V.3. N3. P.417-431. DOI: 10.2478/bf02479272 OpenAlex
New transformation of cycloalkanone acetals by peracids α,ω-dicarboxylic acids synthesis
Open Chemistry. 2005. V.3. N3. P.417-431. DOI: 10.2478/bf02479272 OpenAlex
Идентификаторы БД:
OpenAlex: | W2063275186 |
Цитирование в БД:
БД | Цитирований |
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OpenAlex | 7 |